@article{b1e7674402ce4dd3b1247480cbfce489,
title = "Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)",
keywords = "Homozygotic exon 3 deletion, PARK2, Parkinson's disease",
author = "Kota Sato and Toru Yamashita and Noriko Hatanaka and Mami Takemoto and Nozomi Hishikawa and Yasuyuki Ohta and Koji Abe",
note = "Funding Information: We are grateful to Dr. Hiroyo Yoshino Ph. D (Research Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan) for her important contributions to the genetic diagnosis of PARK2. This work was partly supported by a Grant-in-Aid for Scientific Research (B) 2529320216 , (C) 24591263 and Challenging Research 24659651 , and by Grants-in-Aid from the Research Committees (Mizusawa H, Nakajima I, Nishizawa M, Sasaki H, and Aoki M) from the Ministry of Health, Labour and Welfare of Japan.",
year = "2016",
month = sep,
day = "15",
doi = "10.1016/j.jns.2016.07.004",
language = "English",
volume = "368",
pages = "147--149",
journal = "Journal of the Neurological Sciences",
issn = "0022-510X",
publisher = "Elsevier",
}